在类器官中使用多路形态原筛选产生人类神经多样性。

Neal D Amin, Kevin W Kelley, Jin Hao, Yuki Miura, Genta Narazaki, Tommy Li, Patrick McQueen, Shravanti Kulkarni, Sergey Pavlov, Sergiu P Paşca
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引用次数: 4

摘要

在发育中的神经系统中,形态原编排了显著的细胞多样性的产生。干细胞在体外向特定的神经细胞分化往往依赖于这些信号通路的组合调节。然而,缺乏系统的方法来理解形态导向的分化已经排除了许多神经细胞群体的产生,并且区域规范的一般原则的知识仍然不完整。在这里,我们在培养超过70天的人类神经类器官中开发了14种形态因子的阵列筛选。利用多路RNA测序技术的进步和人类胎儿大脑的注释单细胞参考,我们发现这种筛选方法在神经轴上产生了相当大的区域和细胞类型多样性。通过反卷积形态-细胞类型关系,我们提取了大脑区域规范的设计原则,包括关键形态发生时间窗口和组合,产生一系列具有不同神经递质身份的神经元。调节gaba能神经亚型多样性意外地导致了灵长类特异性中间神经元的衍生。综上所述,这将为人类神经细胞分化的体外形态原图谱提供一个平台,这将为人类的发育、进化和疾病带来新的见解。
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Generating human neural diversity with a multiplexed morphogen screen in organoids.

Morphogens choreograph the generation of remarkable cellular diversity in the developing nervous system. Differentiation of stem cells toward particular neural cell fates in vitro often relies upon combinatorial modulation of these signaling pathways. However, the lack of a systematic approach to understand morphogen-directed differentiation has precluded the generation of many neural cell populations, and knowledge of the general principles of regional specification remain in-complete. Here, we developed an arrayed screen of 14 morphogen modulators in human neural organoids cultured for over 70 days. Leveraging advances in multiplexed RNA sequencing technology and annotated single cell references of the human fetal brain we discovered that this screening approach generated considerable regional and cell type diversity across the neural axis. By deconvoluting morphogen-cell type relationships, we extracted design principles of brain region specification, including critical morphogen timing windows and combinatorics yielding an array of neurons with distinct neuro-transmitter identities. Tuning GABAergic neural subtype diversity unexpectedly led to the derivation of primate-specific interneurons. Taken together, this serves as a platform towards an in vitro morphogen atlas of human neural cell differentiation that will bring insights into human development, evolution, and disease.

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